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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Journal of neurochemistry 92 (2005), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: We sought to determine whether the extracellular compartment contributed to seizure-induced superoxide (O2.−) production and to determine the role of the NADPH oxidase complex as a source of this O2.− production. The translocation of NADPH oxidase subunits (p47phox, p67phox and rac1) was assessed by immunoblot analysis and NADPH-driven O2.− production was measured using 2-(4-hydroxybenzyl)-6-(4-hydroxyphenyl)-8-benzyl-3,7-dihydroimidazo [1,2-α] pyrazin-3-one-enhanced chemiluminescence. Kainate-induced status epilepticus resulted in a time-dependent translocation of NADPH oxidase subunits (p47phox, p67phox and rac-1) from hippocampal cytosol to membrane fractions. Hippocampal membrane fractions from kainate-injected rats showed increased NADPH-driven and diphenylene iodonium-sensitive O2.− production in comparison to vehicle-treated rats. The time-course of kainate-induced NADPH oxidase activation coincided with microglial activation in the rat hippocampus. Finally, kainate-induced neuronal damage and membrane oxygen consumption were inhibited in mice overexpressing extracellular superoxide dismutase. These results suggest that seizure activity activates the membrane NADPH oxidase complex resulting in increased formation of O2.−.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 428 (1984), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 216 (1986), S. 49-54 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The distribution of brush cells in the rat lung was studied using electron microscopic morphometry. Samples were taken from six distinctive anatomical regions. Tissue from the trachea, lobar bronchi, terminal bronchioles, first alveolar duct bifurcations, proximal alveolar regions, and the distal alveolar region were isolated and embedded in Epox 812. Aside from the trachea and the lobar bronchi, the other four regions were isolated from embedded tissue using microdis-section techniques. Electron micrographs taken from thin sections of these samples were analyzed. It was found that brush cells made up 10% of the volume of epithelium covering the first alveolar duct bifurcation. Approximately 2% of the proximal alveolar epithelium, 1.4% of the terminal bronchiolar epithelium, and 3% of the tracheal epithelium were made up of brush cells. No brush-bordered epithelium was found in the lobar bronchi or in the distal alveolar walls. We conclude that brush cells have a distinct spatial location in the lung, being in high concentration in the trachea and in areas where first generation alveolar duets bifurcate. The highest density was on the bifurcation of the first alveolar ducts, and their density decreased radially from this region.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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